http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0293548-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-01
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-365
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00
filingDate 1988-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e53aa91819c88a1a297438981fc17652
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aedc744329e13a653c32f238027562d6
publicationDate 1988-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0293548-A2
titleOfInvention Mono- and diepoxide derivatives of LL-F28249 compounds
abstract The present invention relates to novel mono­C(26,27) and diepoxide C(14,15;26,27) derivatives of LL-F28249α, β, ε, ζ, ϑ and compounds. The LL-F28249 compounds (collectively) are isolates from the fermen­tation broth of Streotomyces cyaneogriseus subspecies noncyanogenus having deposit accession number NRRL­15773. The compounds of this present invention are derived by regioselective epoxidation of 5,23-0,0-bis-­silylated LL-F28249 compounds at low temperature, followed by desilylation. These novel compounds have anthelmintic, insecticidal, ectoparasiticidal, nema­ticidal and acaricidal activity and also are useful intermediates for the preparation of further biologi­cally active compounds. Compositions containing these described derivatives as active ingredients thereof are described.
priorityDate 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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